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Valvular Heart Disease. ADRIEL E. GUERRERO, MD, FPCP, FPCC Training Officer Section of Cardiology, Dept of Medicine The Medical City. Mitral Stenosis. Diagnostic Features of MS @. 2/3 are females; Pure MS are generally rheumatic History: Exertional Dyspnea, PND, Orthopnea and Hemoptysis
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Valvular Heart Disease ADRIEL E. GUERRERO, MD, FPCP, FPCC Training Officer Section of Cardiology, Dept of Medicine The Medical City
Diagnostic Features of MS@ • 2/3 are females; Pure MS are generally rheumatic • History: • Exertional Dyspnea, PND, Orthopnea and Hemoptysis • PE: • Opening snap, loud S1, diastolic rumble at the apex • ECG and Chest Xray: • Evidence of left atrial enlargement with normal left ventricular size; RVH in later stages • 2DECHO
Common Etiologies of MS • Rheumatic Heart Disease • Congenital Heart disease • Congenital MS • Lutembachers syndrome (MS and ASD) • Mitral Annular Calcification (elderly)
Mitral Stenosis@ Pathophysiology Obstruction to LV filling Increase LA pressure RV Failure
Natural History of MS • Pulmonary Hypertension • Fibrous thickening of alveolar and pulmo capillary walls • Thrombi and Emboli • Left atrial appendage • Increased: AF, older patients, reduced CO • Pulmonary Infections, IE,
Natural History of Mitral Stenosis MS - blue MR - purple
Differential Diagnosis of MS • Atrial Septal Defect • RVE and accentuated pulmo markings • Widely split S2 (fixed)VS Opening snap; diastolic flow across the TV • No LAE • Left Atrial Myxoma • Obstructing LA emptying, tumor-plop • Mitral Regurgitation • Systolic murmur; LVH • Aortic Regurgitation (Austin Flint) • Apical middiastolic murmur of AR. Becomes louder on handgrip and decreases with amyl nitrate
Treatment of MS • Penicillin Prophylaxis of B-hemolytic Streptococcal Infections to prevent Rheumatic Fever and IE • Sodium restriction, oral diuretics • Oral Anticoagulation (Warfarin) • INR target 2-3.1 (embolization, permanent AF) • Heart Rate Controlling drugs • To lengthen diastolic LV filling • Digitalis in Atrial Fibrillation; Beta-blockers in sinus rhythm • Nondihydropyridine Calcium Antagonists
Mitral Valvotomy • Indicated in symptomatic patients with isolated MS (<1.0 cm2/m2) • Ideal for mobile, thin leaflets with no or little calcium without extensive subvalvular thickening and with no or mild MR • Open valvotomy – mortality rate is 2% • 50% of all patients require reoperation by 10 years. • Pregnant – carried out if pulmonary congestion occurs despite intensive medical treatment
Mitral Valve Replacement • MS with significant MR • Distorted valves from previous transcatheter or operative manipulation • Operative Mortality is 6% • Long term complications of valve replacement • Overall 10 year survival is 70% • Poor Recovery • Old patients • Marked disability • Depressed Cardiac index
Mitral Regurgitation • Frequent in males • History: • Easy Fatigue then exertional Dyspnea • PE: • Characteristic holosystolic murmur at the apex with radiation to the axilla
Common Etiologies of MR • MV leaflet abnormality • Rheumatic heart disease • Myxomatous alteration (including MVP) • Infective Endocarditis • Mitral annulus dilatation of any cause • Dilated Cardiomyopathy • IHD with dilated LV • Ruptured chordae tendinae • Trauma • Myocardial Infarction • Papillary muscle disorder • Ischemic Heart Disease
Laboratory Examination • La enlargement; RAE maybe present if pulmonary HPN is severe • Atrial Fibrillation • LVH • ECG • 2DECHO – most accurate non-invasive technique • CXR – LAE and LVE
Medical Treatment for MR • Restrict Physical activities • Reduce sodium intake and enhance sodium excretion (diuretics) • Increase forward cardiac output • Vasodilators (ACEI) and digitalis • Anticoagulants and leg binders to decrease likelihood of venous thrombi and pulmonary emboli • Endocarditis prophylaxis
Surgical Treatment of MR • Non-surgical candidates: asymptomatic, or exercise limited to strenuous exertion, normal LV function • Surgery for severe MR even if asymptomatic or when LV dysfunction is progressive (declining <60%) and/or LV ESD on echo is >45mm • MV replacement for markedly shrunken, deformed, calcified leaflets • MV repair (reconstruction) with annuloplasty • Lessens problem on long term anticoagulation and thromboembolism • For ruptured chordae, annular dilatation and IE • Not suitable for Mr due to myxomatous degeneration and patients with calcified annulus
Late Survival Rates after Surgical Correction in MR (pre-op EF)
Mitral Valve Prolapse • Barlow’s syndrome, floppy-valve syndrome, systolic click-murmur syndrome, billowing mitral leaflet syndrome • Excessive or redundant mitral leaflet tissue. Posterior MV leaflet is more affected than the AMVL • May lead to excessive stress on the papillary muscles leading to dysfunction. Rupture of chordae tendineae with progressive annular dilatation and calcification • Ventricular arrythmias
Clinical Features • Females (14-30 years old) • Clinical course is often benign • Increased familial incidence – autosomal dominant • Most common cause of isolated severe MR requiring surgical treatment in North America • Arrythmias (PVCs, SVTs, VTs) – palpitations, lightheadedness and syncope. Sudden death is rare • Chest pain substernal, prolonged, unrelated to exertion
Mitral Valve Prolapse Mismatch between elongated MV and LV cavity
Laboratory Exams • ECG – non specific STTW changes, PVCs • Echo – demonstrates systolic displacement of MVL and quantifies Mitral Regurgitation and LV function
Treatment of MVP • IE prophylaxis • Beta-blockers sometimes relieve chest pain • For severe symptomatic MR, MV repair or rarely replacement is indicated • Antiplatelets for patients with TIA, anticoagulation if recurrent TIAs
Survival Rates of MVP patients at baseline risk factors Primary Risk Factors Mod-severe MR; EF <50% Secondary Risk Factors Mild-mod MR; LA > 40 Flail leaflet; AF; age > 50
Aortic Stenosis • 80% with symptomatic AS are males • Age-related degenerative calcific AS – most common cause of AS in Adults
Common Etiologies of AS • Valvular (90% of all cases) • Rheumatic heart disease • Degenerative calcification (elderly) • Bicuspid AV stenosis/ Congenital heart disease • Subvalvular (9%) • Hypertrophic Obstructive Cardiomyopathy (HOCM) • Discrete • Supravalvular (<1%) • Infancy
Aortic Stenosis • History: • Cardinal symptoms • Exertional Dyspnea • Angina Pectoris • Syncope • PE • Carotid upstroke slowly rising and reduced in amplitude in severe cases; Systolic ejection murmur radiating to the carotid arteries
Laboratory Exam • LV hypertrophy is the key finding • ECG • 2DECHO – estimate valve area, LV size and function • Cardiac catheterization • Presence or absence of concomittant CAD
Natural History of Severe AS • Death most commonly occurs in the 7th and 8th decade • Average time from onset of symptoms to death: • Angina – 3 years • Syncope – 3 years • Heart Failure – 1.5 – 2 years • Sudden death 10-20% in AS patients 60 years old and above